Canonical Allele Identifier: CA2668620438

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179203910-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203910A>C , CM000665.2:g.179203910A>C	GRCh38
NC_000003.11:g.178921698A>C , CM000665.1:g.178921698A>C	GRCh37
NC_000003.10:g.180404392A>C	NCBI36
NG_012113.2:g.60388A>C , LRG_310:g.60388A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1059+121A>C MANE Select	ENSP00000263967.3:n.1059+121A>C
ENST00000643187.1:c.1059+121A>C	ENSP00000493507.1:n.1059+121A>C
ENST00000674534.1:n.813+121A>C
ENST00000675467.1:n.3866+121A>C
ENST00000675786.1:c.1059+121A>C	ENSP00000502323.1:n.1059+121A>C
ENST00000263967.3:c.1059+121A>C	ENSP00000263967.3:n.1059+121A>C
NM_006218.2:c.1059+121A>C , LRG_310t1:c.1059+121A>C	NP_006209.2:n.1059+121A>C
XM_006713658.2:c.1059+121A>C	XP_006713721.1:n.1059+121A>C
XM_011512894.1:c.1059+121A>C	XP_011511196.1:n.1059+121A>C
NM_006218.3:c.1059+121A>C	NP_006209.2:n.1059+121A>C
XM_006713658.4:c.1059+121A>C	XP_006713721.1:n.1059+121A>C
XM_011512894.2:c.1059+121A>C	XP_011511196.1:n.1059+121A>C
NM_006218.4:c.1059+121A>C MANE Select	NP_006209.2:n.1059+121A>C